Purpose: To describe the distribution of ocular disorders in patients with a family history of consanguinity presenting to a multi-tier ophthalmology hospital network in India. Methods: This cross-sectional hospital-based study included 2,805,267 new patients presenting between August 2010 and April 2021. Patients with a family history of consanguinity were included as cases. The sociodemographic and clinical data were collected using an electronic medical record system. Results: Overall, 20,445 (0.73%) new patients were documented to have a family history of consanguinity. The prevalence rates were 4.04% in children (age: <16 years) and 0.21% in adults. The mean age of the patients was 11.87 ± 11.06 years. The majority of the patients were...
Abstract Background and Objective: Consanguinity increases the incidence of genetic disorders. The ...
Introduction: Thalassemia is a blood disorder characterized by defective alpha or beta chain synthes...
PURPOSE: Oculocutaneous albinism (OCA) is a group of autosomal recessive disorders characterized by ...
Purpose: To determine the prevalence of consanguinity and its potential associations with eye diseas...
Purpose: Big data is the new gold, especially in health care. Advances in collecting and processing ...
Purpose: To describe the clinical profile of patients with ocular Calotropis poisoning presenting to...
Background: Congenital Heart Diseases (CHDs) are the commonest single group of congenital abnormalit...
Aim: To study the impact of consanguinity on frequency pattern of fertility and congenital malformat...
Objective: To assess the pattern of eye diseases in children presenting at Basic Health Unit, Hassan...
Aim: To analyze various ocular diseases leading to permanent visual handicap in a district situated ...
Purpose: To study the demographic profile, severity and causes of visual impairment among registered...
Background: Ocular Morbidities with its economic and social consequences, represents an important pu...
Purpose: To measure the proportion of people with major ophthalmic and retinal disorders in the trib...
Background: The aim of the study was to determine the various types of congenital or acquired disord...
Leber congenital amaurosis (LCA) and retinitis pigmentosa (RP) are retinal degenerative diseases whi...
Abstract Background and Objective: Consanguinity increases the incidence of genetic disorders. The ...
Introduction: Thalassemia is a blood disorder characterized by defective alpha or beta chain synthes...
PURPOSE: Oculocutaneous albinism (OCA) is a group of autosomal recessive disorders characterized by ...
Purpose: To determine the prevalence of consanguinity and its potential associations with eye diseas...
Purpose: Big data is the new gold, especially in health care. Advances in collecting and processing ...
Purpose: To describe the clinical profile of patients with ocular Calotropis poisoning presenting to...
Background: Congenital Heart Diseases (CHDs) are the commonest single group of congenital abnormalit...
Aim: To study the impact of consanguinity on frequency pattern of fertility and congenital malformat...
Objective: To assess the pattern of eye diseases in children presenting at Basic Health Unit, Hassan...
Aim: To analyze various ocular diseases leading to permanent visual handicap in a district situated ...
Purpose: To study the demographic profile, severity and causes of visual impairment among registered...
Background: Ocular Morbidities with its economic and social consequences, represents an important pu...
Purpose: To measure the proportion of people with major ophthalmic and retinal disorders in the trib...
Background: The aim of the study was to determine the various types of congenital or acquired disord...
Leber congenital amaurosis (LCA) and retinitis pigmentosa (RP) are retinal degenerative diseases whi...
Abstract Background and Objective: Consanguinity increases the incidence of genetic disorders. The ...
Introduction: Thalassemia is a blood disorder characterized by defective alpha or beta chain synthes...
PURPOSE: Oculocutaneous albinism (OCA) is a group of autosomal recessive disorders characterized by ...